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Marathon of Hope Cancer Centres Network Study for Ontario (MOHCCN-O)

Marathon of Hope Cancer Centres Network Study for Ontario (MOHCCN-O)

Recruiting
18 years and older
All
Phase N/A

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Overview

The Marathon of Hope Cancer Centres Network (MOHCCN) is a national network of cancer centres that pursue collaborative cancer research in precision medicine (an emerging approach for disease treatment and prevention that considers individual variability in DNA, environment and lifestyle) to accelerate the discovery of innovations and improve the health outcomes for cancer patients

Description

The purpose of this study is to use evolving technologies such as genomics and artificial intelligence to study cancer so that the right treatment can be given to the right patient, at the right time. Approximately 15,000 participants will take part in the greater MOHCCN study across Canada in the first 5 years, and ultimately the goal is to enroll up to 100,000 over next 10 years.

Eligibility

Inclusion Criteria:

  1. Patients with histological and/or cytological confirmation of blood or solid tumor malignancies. For tumour types where pre-surgical biopsy is not routinely performed to confirm a pathologic diagnosis of cancer, patients may consent to this protocol, but eligibility must be confirmed after pathology is finalized demonstrating presence of malignancy
  2. All patients must be able to satisfy the required minimum data elements for the 15k gold standard cohort through:
    1. Already existing data that satisfies the minimal requirements of a gold standard case (refer to Table 1)
    2. Have sufficient biospecimens (tumor and/or blood samples) available for more comprehensive molecular and immunophenotypic characterization
  3. Patients who do not satisfy the required minimum data elements but would like to participate, maybe requested to donate blood and undergo a fresh biopsy if the archived Formalin-fixed paraffin-embedded (FFPE) samples are not available, or in cases where a fresh tumor biopsy is deemed necessary for molecular profiling.
  4. Participating patients must agree to share their anonymized clinical and genomic data

Exclusion Criteria:

None.

Study details
    Breast Cancer
    Colorectal Cancer
    Pancreas Cancer
    Kidney Cancer
    Prostate Cancer
    Ovary Cancer
    Head and Neck Cancer
    Leukemia
    Lymphoma
    Lung Cancer
    Melanoma
    Solid Tumor

NCT05403177

University Health Network, Toronto

15 May 2026

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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